Ionotropic glutamate receptor NMDA type subunit 1 dysregulation

Synonym(s)
- Autosomal dominant intellectual disability type 8,
- neurodevelopmental disorder with or without hyperkinetic movements and seizures
Type

Disease
External link(s)
- IEMbase
Gene
- GRIN1 / Glutamate Ionotropic Receptor NMDA Type Subunit 1
  9q34.3
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Glutamate receptor subunit NMDA1
Disease group(s)
- 23.3 Glutamate neurotransmitter disorders